Linked Data
dbSNP Id:
rs139021858
ExAC:
12:102179828 G / C
gnomAD v2:
12-102179828-G-C
gnomAD v4:
12-101786050-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.101786050G>C , CM000674.2:g.101786050G>C | GRCh38 |
| NC_000012.11:g.102179828G>C , CM000674.1:g.102179828G>C | GRCh37 |
| NC_000012.10:g.100703959G>C | NCBI36 |
| NG_021243.1:g.49818C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000299314.12:c.533C>G MANE Select | ENSP00000299314.7:p.Thr178Ser | |
| ENST00000299314.11:c.533C>G | ENSP00000299314.7:p.Thr178Ser | |
| ENST00000549940.5:c.533C>G | ENSP00000449150.1:p.Thr178Ser | |
| ENST00000550352.1:n.327C>G | ||
| ENST00000552681.1:c.167C>G | ENSP00000449217.1:p.Thr56Ser | |
| NM_024312.4:c.533C>G | NP_077288.2:p.Thr178Ser | |
| XM_006719593.2:c.533C>G | XP_006719656.1:p.Thr178Ser | |
| XM_011538731.1:c.452C>G | XP_011537033.1:p.Thr151Ser | |
| XM_006719593.3:c.533C>G | XP_006719656.1:p.Thr178Ser | |
| XM_011538731.2:c.452C>G | XP_011537033.1:p.Thr151Ser | |
| XM_017019961.1:c.317C>G | XP_016875450.1:p.Thr106Ser | |
| XM_017019962.2:c.-818C>G | XP_016875451.1:n.-818C>G | |
| NM_024312.5:c.533C>G MANE Select | NP_077288.2:p.Thr178Ser |